Lecture 16 Flashcards

(27 cards)

1
Q

what is a linkage group

A

all of the genes on a given chromosome are said to be linked or to belong to the same linkage group

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2
Q

what is linkage equilibrium?

A

when loci of different chromosomes hae 50% chance of being packaged together in the same gamete. essentially the equal chance that the diff loci on different chromosomes have to be packaged together

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3
Q

what happens to loci on the same chromosome?

A

because of meiosis and genetic recombination, alleles sometimes get moves from one copy of a chromosome to another

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4
Q

what does the probability of loci being swapped by recombination depend on?

A

depends on the distance between them

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4
Q

Loci far apart are ________ linked

A

less

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5
Q

loci close together are _________ linked

A

tightly

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6
Q

what happens if loci are exact opposite ends of the chromosome?

A
  • the loci will often recombine
  • all gamete types are equally likely
  • maximum possinle rate of 0.5
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7
Q

what happens if the loci are so closely linked?

A
  • recombination never occurs
  • the rate is 0
  • the minimum possinle value the alleles at the two loci are inherited together
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8
Q

what is genetic linkage?

A

refers to the linkage of multiple locu due to the fact they are transmitted through meiosis together

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9
Q

what is linkage disequilibrium (D)?

A
  • refers to the relationship between the alleles at different loci
  • this may due to physical genetic linkage but does not necessarily always be this
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10
Q

when are two loci said to be in linkage disequilibrium?

A
  • D>0
  • when knowing the allele at one locus enables you to predict what the allele at the oher locus likely is
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11
Q

what is the maximum linkage?

A

D=0.25 (or -0.25)

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12
Q

what is no linkage?

A

D=0

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13
Q

How do we calculate how different the observed frequency of one genotype is compared to the expected

A

D=Observed-Expected

D=extent of linkage disequilibrium
Observed= observed frequency
Expected= expected freuqnecy if the individuals of the two loci are segregating loci independently (linkage equilibrium)

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14
Q

what does it mean when D=0?

A

zero means no linkage disequilbrium (fully recombining)

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15
Q

what eliminates linkage disequilibrium from a population?

A
  • linkage is broken down by recombination
  • crossing over during meiosis breaks up old combinations of alleles and creates new combinations
  • this takes MORE than a single generation (the process of breaking up disequilbrium between two loci)
16
Q

What are the causes of linkage disequilibrium?

A
  • physical linkage of locus A and locus B on same chromosome
  • natural selection (favoring one combination over another)
  • gene flow (population structure- AABB individuals arriving in aabb populations)
  • assortive mating (AB and AB mate, and ab and ab mate)
17
Q

how can we use linkage disequilibrium?

A
  • sudying migration or dispersal between populations with different gene frequencies or between species
  • reconstructing the history of genes and pop.
  • indentifying alleles under selection
  • mapping of genes of interest
18
Q

Why would we map genes of underlying traits?

A
  • to study the number of genomic regions that influence a quantitative trait
  • the magnitude of their effect
  • their location in the genome
19
Q

what is quantitative trait locus (QTL)?

A
  • a region of the genome that is correlated with variation in a phenotypic trait
  • the region contains the genes (and other genes linked to it) that contribute to population differences in a phenotype
20
Q

What does QTL use?

A

uses an experiemental cross to create linkage disequilibrium (because only one generation of recombination), and then uses moleculars markers throughout the genome to find the regions where there is statistical association between the phenotype of interest and molecular markers

21
Q

why is QTL analysis helpful?

A

since each region of a chromosome contributes genes that may or may not affect the trait of interest, by recombining the chromosomes one can find the regions that contribute to the phenotype

22
Q

can we do QTL analysis in humans?

A

no, so we use different strategies

23
Q

what is genome wide association studies (GWAS)?

A
  • QTL analysis but for humans
  • looks for correlations between the genotypes at genetic markers and phenotypic traits
  • use existing linkage disequilibrium to find association (because recombination is slowo to break down combination of alleles)
24
what does genome wide association scan for?
GWAS scan for genetic loci associated with disease risk
25
how can we use GWAS to scan for a trait?
* compare frequencies of alleles (SNPs) at each position of the genome for the groups with or without the trait * at casual loci (and the areas around it that are in linkage disequilibrium) will find more differences between the groups than the rest of the genome * would need to be careful about defining the groups tho!!
26
true or false: linkage disequilibrium can mean that multiple genes evolve together (and this can aid in adaptation)
true